ClinVar Genomic variation as it relates to human health
NM_173491.4(LSM11):c.208G>A (p.Gly70Ser)
Germline
Classification
(1)
Likely benign
no assertion criteria provided
Somatic
No data submitted for somatic clinical impact
Somatic
No data submitted for oncogenicity
Genes
Gene | OMIM | ClinGen Gene Dosage Sensitivity Curation | Variation Viewer | Related variants | ||
---|---|---|---|---|---|---|
HI score | TS score | Within gene | All | |||
LOC129995145 | - | - | - | GRCh38 | - | 24 |
LSM11 | - | - |
GRCh38 GRCh37 |
22 | 59 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
LSM11-related disorder
|
Likely benign (1) |
|
May 23, 2022 | RCV003917094.2 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Oct 08, 2024